| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:18322467-18322616 | Common:2; Rare:63 | ||||
| chr11:18526828-18526972 | Rare:70 | ||||
| chr11:18588672-18588860 | Common:2; Rare:63 | ||||
| chr11:19777570-19777815 | Common:1; Rare:55 | ||||
| chr11:22625518-22625601 | Rare:41; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:22625808-22626002 | Common:2; Rare:68; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:22829357-22829422 | Common:1; Rare:18 | ||||
| chr11:26572134-26572466 | Rare:56 | ||||
| chr11:26994001-26994127 | Rare:19 | ||||
| chr11:27363090-27363346 | Rare:114 | ||||
| chr11:27506739-27506863 | Common:1; Rare:51 | ||||
| chr11:28108181-28108421 | Common:1; Rare:74 | ||||
| chr11:30584003-30584150 | Rare:39 | ||||
| chr11:31369731-31369882 | Rare:45 | ||||
| chr11:31509561-31509806 | Common:1; Rare:81 |